Are you launching or exporting a medical device, wellness product, or cosmetic item in the UK, US, or EU?
Failing to meet strict regulatory guidelines can lead to customs seizures, store bans, or heavy penalties. I deliver end-to-end medical device regulatory compliance to get your products legally certified and market-ready.
Services Provided in This Gig:
- MHRA Registration: Registration of devices with the UK Medicines and Healthcare products Regulatory Agency.
- UKCA Certification: Guidance, Declaration of Conformity, and technical file alignment for Great Britain.
- FDA Compliance: FDA Owner/Operator Registration, Device Listing, 510(k) guidance, and US Agent setup.
- EU MDR Compliance (2017/745): Clinical Evaluation Reports (CER), Risk Management File (ISO 14971), GSPR mapping, and Technical File compilation.
Why Choose Me?
- 100% Compliance guarantee aligned with the latest EU MDR/UKCA directives.
- Proven experience with Class I, Class IIa, and Class IIb medical devices & IVDs.
- Clear communication and fast turnaround times.